Premium
A genetic variant of pri‐miR ‐182 may impact the risk for the onset of multiple sclerosis in the Iranian population
Author(s) -
Najafi Nadia,
Peymani Maryam
Publication year - 2020
Publication title -
american journal of human biology
Language(s) - English
Resource type - Journals
SCImago Journal Rank - 0.559
H-Index - 81
eISSN - 1520-6300
pISSN - 1042-0533
DOI - 10.1002/ajhb.23415
Subject(s) - genotype , multiple sclerosis , allele , single nucleotide polymorphism , disease , genetic association , population , autoimmune disease , polymorphism (computer science) , allele frequency , immunology , genetics , medicine , biology , gene , environmental health
Background Multiple sclerosis (MS) is the most common autoimmune disease of the central nervous system affecting young adults. SNPs can be used as genetic biomarkers to identify disease‐related genes such as MS. Moreover, SNPs can be considered as important determinants for an increased risk of autoimmune diseases such as MS. Studies have shown that miR‐182 is of importance in Treg cell development and function as critical regulators in autoimmune disease. So far, no study has been conducted to investigate the association between rs4541843 polymorphism in pri‐miR‐182 and MS. In the present study, we assessed the frequency of rs4541843 different alleles and genotypes and their association with MS risk in Iranian population. Methods The rs4541843 was genotyped in 81 patients with MS and 89 healthy subjects, using the PCR‐RFLP method. The frequency of alleles and genotypes and the association of this polymorphism with MS risk and the gender of the patients was then statistically analyzed. Results Statistical analysis showed the protective role of AA genotype against MS risk ( P = .031, OR = 0.348) while there was no significance correlation between the frequency of rs4541843 different alleles and the other genotypes. Conclusion Our findings illustrated that the pri‐miR‐182 rs4541843 G>A polymorphism is associated with the risk of MS in Isfahan population. However, additional large‐scale association studies in various ethnicities and more molecular studies are necessary to elaborate our findings.